ClearanceBrief
510(k) K111438 ยท DPS Electrocardiograph

REKA E100

ApplicantReka Pte, Ltd., Summerville SC, US
DecisionSubstantially Equivalent, Sep 12, 2011
ReceivedMay 24, 2011
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K111438

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.